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Showing 1 to 12 of 387 entries
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Computed tomography scanning and stroke mortality in an urban medical unit in Cameroon.

eNeurologicalSci

Lekoubou A, Nkoke C, Dudzie A, Kengne AP.
PMID: 29473054
eNeurologicalSci. 2016 Jan 26;2:3-7. doi: 10.1016/j.ensci.2016.01.003. eCollection 2016 Mar.

BACKGROUND: Despite the increasing availability of head computerized tomography (CT) in resource-limited settings, it is unclear if brain-imaging-based diagnosis of stroke affects the outcomes in the absence of dedicated structures for acute stroke management.OBJECTIVES: In a major referral hospital...

Late-onset myasthenia gravis is predisposed to become generalized in the elderly.

eNeurologicalSci

Sakai W, Matsui N, Ishida M, Furukawa T, Miyazaki Y, Fujita K, Miyamoto R, Yamamoto N, Sako W, Sato K, Kondo K, Nishida Y, Mitsui T, Izumi Y, Kaji R.
PMID: 29473057
eNeurologicalSci. 2016 Feb 11;2:17-20. doi: 10.1016/j.ensci.2016.02.004. eCollection 2016 Mar.

OBJECTIVE: The continuous increase in the number of patients presenting with late-onset myasthenia gravis (LOMG) underscores the need for a better understanding of the clinical course and the establishment of an optimal therapeutic strategy. We aimed to clarify factors...

Functional validation and expression analysis of myotubes converted from skin fibroblasts using a simple direct reprogramming strategy.

eNeurologicalSci

Horio F, Sakurai H, Ohsawa Y, Nakano S, Matsukura M, Fujii I.
PMID: 29260008
eNeurologicalSci. 2016 Nov 03;6:9-15. doi: 10.1016/j.ensci.2016.11.002. eCollection 2017 Mar.

Previously, we reported that MyoD, a master gene for myogenic cells, could efficiently convert primary skin fibroblasts into myoblasts and myotubes, thereby effecting direct reprogramming. In this study, we further demonstrated that MyoD-expressing primary fibroblasts displayed rapid movement in...

Time-courses of plasma IL-6 and HMGB-1 reflect initial severity of clinical presentation but do not predict poor neurologic outcome following subarachnoid hemorrhage.

eNeurologicalSci

Kiiski H, Långsjö J, Tenhunen J, Ala-Peijari M, Huhtala H, Hämäläinen M, Moilanen E, Öhman J, Peltola J.
PMID: 29260012
eNeurologicalSci. 2016 Dec 02;6:55-62. doi: 10.1016/j.ensci.2016.11.010. eCollection 2017 Mar.

OBJECTIVE: Patients with aneurysmal subarachnoid hemorrhage (aSAH) experience high mortality and morbidity. Neuroinflammation causes brain damage expansion after aSAH. Due to the complexity of the inflammatory response multiple biomarkers are needed to evaluate its' progression. We studied inflammatory process...

Popular stroke knowledge in Brazil: A multicenter survey during "World Stroke Day".

eNeurologicalSci

Gomes ABAGR, Henrique M, Schoeps VA, Santos MMSA, Pellegrinelli A, de Matos BP, Kubota GT, Araújo HA, da Silva LSAC, de Paula Leite Battisti F, Kubota BY, Ferreira AC, Pellegrino MP, de Andrade Prado R, Abrahm R, Gagliardi VDB, Simis M, Gagliardi RJ.
PMID: 29260013
eNeurologicalSci. 2016 Dec 16;6:63-67. doi: 10.1016/j.ensci.2016.12.002. eCollection 2017 Mar.

CONTEXT AND OBJECTIVE: Cerebrovascular disease is one of the most important causes of death and disability worldwide. The patient's inability to identify the warning signs of stroke substantially delays the search for emergency services, which is related directly to...

Evolution into moyamoya disease in an infant with internal carotid artery aneurysms.

eNeurologicalSci

Tanaka R, Takahashi S, Okano S, Okayama A, Suzuki N, Kure S, Azuma H.
PMID: 29260015
eNeurologicalSci. 2017 Jan 31;6:80-82. doi: 10.1016/j.ensci.2017.01.002. eCollection 2017 Mar.

INTRODUCTION: Moyamoya disease (MMD) is characterized by progressive stenosis and occlusion in the terminal portion of both internal carotid arteries (ICAs) and the formation of an abnormal vascular network. Because of the fragile structure of the collateral vessels, MMD...

Prosopometamorphopsia and alexia following left splenial corpus callosum infarction: Case report and literature review.

eNeurologicalSci

McCarty CW, Gordon GM, Walker A, Delio P, Kolarczyk RA, Pieramici DJ.
PMID: 29260005
eNeurologicalSci. 2016 Aug 20;6:1-3. doi: 10.1016/j.ensci.2016.08.002. eCollection 2017 Mar.

BACKGROUND: Lesions to the posterior section of the corpus callosum, called the splenium, and the immediate area have been separately associated with perceived visual distortions of the face (prosopometamorphopsia) or difficulty reading (alexia).CASE REPORT: This case report describes a...

The utility of ultrasound in showing a unique cause of posterior interosseous nerve syndrome.

eNeurologicalSci

Soh D, Cappelen-Smith C, Korber J, Heath T, Cordato D.
PMID: 29260034
eNeurologicalSci. 2017 Jul 20;8:34-35. doi: 10.1016/j.ensci.2017.07.002. eCollection 2017 Sep.

No abstract available.

Eculizumab improved weakness and taste disorder in thymoma-associated generalized myasthenia gravis with anti-striational antibodies: A case report.

eNeurologicalSci

Amano E, Otsu S, Suzuki S, Machida A.
PMID: 30705973
eNeurologicalSci. 2019 Jan 07;14:72-73. doi: 10.1016/j.ensci.2019.01.006. eCollection 2019 Mar.

No abstract available.

Differential expression of miRNA 155 and miRNA 146a in Parkinson's disease patients.

eNeurologicalSci

Caggiu E, Paulus K, Mameli G, Arru G, Sechi GP, Sechi LA.
PMID: 30255159
eNeurologicalSci. 2018 Sep 14;13:1-4. doi: 10.1016/j.ensci.2018.09.002. eCollection 2018 Dec.

Parkinson's disease is a neurodegenerative disorder and its etiology is unknown, numerous studies show how different environmental factors can influence the development of disease. miRNAs are involved in several pathologies and their dysregulation contribute to different pathologies, also in...

Carpal tunnel syndrome observed after an arbovirus infection: A preliminary case series report.

eNeurologicalSci

de Aquino Neves EL, Nunes PS.
PMID: 30211326
eNeurologicalSci. 2018 Aug 21;12:31-33. doi: 10.1016/j.ensci.2018.08.004. eCollection 2018 Sep.

PURPOSE: Report a case series study of individuals who, after having a suspected arboviral disease during an epidemic outbreak in north-eastern Brazil, presented symptoms of acroparesthesia.METHODS: A retrospective evaluation of patients with acroparesthesia undertaken between December 2015 and October...

Recurrent autonomic and sensory neuropathy in a patient with anti-ganglionic acetylcholine receptor antibodies.

eNeurologicalSci

Watanabe E, Fujita T, Shimono M, Koike H, Yasumoto S, Hirose S.
PMID: 30211328
eNeurologicalSci. 2018 Aug 23;12:36-38. doi: 10.1016/j.ensci.2018.08.001. eCollection 2018 Sep.

We report a case of recurrent neuropathy with predominant autonomic and sensory involvement whose serum was positive for anti-ganglionic acetylcholine receptor (anti-gAChR) antibodies, a diagnostic marker of autoimmune autonomic ganglionopathy. An 11-year-old girl complained of numbness and limb pain...

Showing 1 to 12 of 387 entries